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首页> 外文期刊>Journal of cellular and molecular medicine. >Stimulated by retinoic acid gene 8 (STRA8) interacts with the germ cell specific bHLH factor SOHLH1 and represses c‐KIT expression in vitro
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Stimulated by retinoic acid gene 8 (STRA8) interacts with the germ cell specific bHLH factor SOHLH1 and represses c‐KIT expression in vitro

机译:通过视黄酸基因8(STRA8)刺激与生殖细胞特异性BHLH因子SOHLH1相互作用并在体外压制C-kit表达

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STRA8 (Stimulated by Retinoic Acid Gene 8) controls the crucial decision of germ cells to engage meiotic division up and down‐regulating genes involved in the meiotic programme. It has been proven as an amplifier of genes involved in cell cycle control and chromosome events, however, how STRA8 functions as negative regulator are not well understood. In this study, we demonstrate that STRA8 can interact with itself and with other basic Helix‐Loop‐Helix (bHLH) transcription factors through its HLH domain and that this domain is important for its ability to negatively interfere with the Ebox‐mediated transcriptional activity of bHLH transcription factors. Significantly, we show that STRA8 interacts with TCF3/E47, a class I bHLH transcription factors, and with SOHLH1, a gonadal‐specific bHLH, in male germ cells obtained from prepuberal mouse testis. We demonstrated that STRA8, indirectly, is able to exert a negative control on the SOHLH1‐dependent stimulation of c‐KIT expression in late differentiating spermatogonia and preleptotene spermatocytes. Although part of this results were obtained only ‘in vitro’, they support the notion that STRA8 interacting with different transcription factors, besides its established role as ‘amplifier’ of meiotic programme, is able to finely modulate the balance between spermatogonia proliferation, differentiation and acquisition of meiotic competence.
机译:SRA8(由视黄酸基因8刺激)控制生殖细胞的关键决定,从而从减少人民计划中参与患有减数分裂的降低和下调基因。已被证明是参与细胞周期控制和染色体事件的基因的放大器,但是,STR8功能如何作为负调节器尚不清楚。在这项研究中,我们证明STRA8可以通过其HLH结构域与其他基本的螺旋环 - 螺旋(BHLH)转录因子相互作用,并且该领域对于其对其产生的能力产生负面影响的能力是重要的BHLH转录因子。值得注意的是,我们表明SRA8与TCF3 / E47,I类BHLH转录因子和SOHLH1相互作用,并且在由Prepubal Mouse Testis获得的男性生殖细胞中具有Gonadal特异性的BHLH。我们展示了STRA8,间接地,能够对晚期分化精子和前肽精子细胞的SAHLH1依赖性刺激对C-kit表达的刺激进行负面控制。尽管该结果的一部分仅获得“体外”,但它们支持STRA8与不同转录因子相互作用的观念,除了其作为“降低人”计划的“放大器”的作用,能够精细调节精子增殖,分化和分化之间的平衡收购减数分裂能力。

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